Canonical Allele Identifier: CA1200666993

Gene: NAXE

Linked Data

• dbSNP Id: rs1677361092

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592554_156592562del , CM000663.2:g.156592554_156592562del	GRCh38
NC_000001.10:g.156562346_156562354del , CM000663.1:g.156562346_156562354del	GRCh37
NC_000001.9:g.154828970_154828978del	NCBI36
NG_052542.1:g.5789_5797del

Transcript Alleles

HGVS	Amino-acid change
ENST00000368235.8:c.403-3_408del
ENST00000467374.2:n.510_518del
ENST00000679369.1:c.292-3_297del
ENST00000679649.1:n.442-3_447del
ENST00000679702.1:c.403-3_408del
ENST00000679913.1:n.607-3_612del
ENST00000680004.1:c.403-3_408del
ENST00000680087.1:c.403-3_408del
ENST00000680269.1:c.403-3_408del
ENST00000680529.1:n.587-3_592del
ENST00000680661.1:c.403-3_408del
ENST00000681054.1:c.403-3_408del
ENST00000681523.1:c.403-3_408del
ENST00000681645.1:n.442-3_447del
ENST00000681734.1:c.403-3_408del
ENST00000681825.1:n.207-3_212del
ENST00000681922.1:n.442-3_447del
ENST00000368233.3:c.403-3_408del
ENST00000368234.7:c.403-3_408del
ENST00000368235.7:c.403-3_408del
ENST00000467374.1:n.312-3_317del
NM_144772.2:c.403-3_408del
XM_017000319.2:c.403-3_408del
NM_144772.3:c.403-3_408del